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FDA 510(k)

DEFIBRILLATOR VPD 545

K-Number: K831056 · 1983-04-28

ApplicantLife Science Instrumentation, Inc.
Decision Date1983-04-28
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DEFIBRILLATOR VPD 545 is the device name listed in this FDA 510(k) record. The listed applicant is Life Science Instrumentation, Inc.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K831056. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEFIBRILLATOR VPD 545?

DEFIBRILLATOR VPD 545 is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Life Science Instrumentation, Inc.. The 510(k) number is K831056.

When did DEFIBRILLATOR VPD 545 receive FDA 510(k) clearance?

DEFIBRILLATOR VPD 545 received FDA 510(k) clearance on 1983-04-28, under 510(k) number K831056.

Who is the listed applicant for DEFIBRILLATOR VPD 545?

The FDA 510(k) record lists Life Science Instrumentation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEFIBRILLATOR VPD 545?

The FDA product code for DEFIBRILLATOR VPD 545 is LDD.

Related Clinical Trials

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Other records listing Life Science Instrumentation, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K850812EMERGIPACE - EXTERNAL PACEMAKERK842037LS 5K843396LS-260G MONITOR/RECORDER & DEFIBILLATORK840246MINI-DEFIBRILLATOR 280/4K822617VPD540 DEFIBRILLATORK822616LS6 ARRYTHMIA DISCRIMINATOR

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Related Devices (Code: LDD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K203231Switched Internal PaddlesPhilips North America, LLCK200849Tempus LS - ManualRemote Diagnostic Technologies, Ltd. A Philips CompanyK182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitorsPhysio-Control, Inc.K103651CARDIOMEDCardio Medical Products, Inc.K103783EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRICFiab SpaK103334CARDIO MEDCardio Medical Products, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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